CRISPR and Gene Editing
CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) technology has revolutionized gene editing, offering precise and efficient ways to modify DNA. In stem cell research, it enables targeted genetic corrections, disease modeling, and the development of personalized therapies. By leveraging CRISPR, researchers are advancing regenerative medicine, genetic disease treatment, and creating improved stem cell models for drug discovery. The potential for CRISPR in stem cell therapies is immense, driving innovations in personalized medicine and transformative healthcare solutions
Related Conference of CRISPR and Gene Editing
March 09-10, 2026
21th World Congress on Tissue Engineering Regenerative Medicine and Stem Cell Research
Singapore City, Singapore
June 18-19, 2026
16th International Conference on Human Genetics and Genetic Diseases
Singapore City, Singapore
June 18-19, 2026
19th International Conference on Genomics & Pharmacogenomics
Singapore City, Singapore
CRISPR and Gene Editing Conference Speakers
Recommended Sessions
- Dental Stem Cells
- Adult Stem Cells
- AI in Stem Cell Research
- Allogeneic Stem Cell Therapies
- Autologous Stem Cells Therapies
- Biotech Innovations
- Cancer Stem Cells
- Clinical Trials
- CRISPR and Gene Editing
- Nanotechnology and Stem Cells
- Neural Stem Cells
- Organoids Technology
- Pluripotent Stem Cells
- Stem Cell Banking and Preservation
- Stem Cell Bioprocessing
- Stem Cell Gene Therapy
- Stem Cell Therapy
- Stem Cell-Based Immunotherapies
- Stem Cells in Oral Health
- Tissue Engineering
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